SG188286A1 - Crystalline (r) - (e) -2- (4- (2- (5- (1- (3, 5 -dichloropyridin-4 -yl) ethoxy) - 1h - indazol - 3 - yl) vinyl) -1 h- pyrazol- 1 -yl) ethanol and its use as fgfr inhibitor - Google Patents

Crystalline (r) - (e) -2- (4- (2- (5- (1- (3, 5 -dichloropyridin-4 -yl) ethoxy) - 1h - indazol - 3 - yl) vinyl) -1 h- pyrazol- 1 -yl) ethanol and its use as fgfr inhibitor Download PDF

Info

Publication number
SG188286A1
SG188286A1 SG2013013743A SG2013013743A SG188286A1 SG 188286 A1 SG188286 A1 SG 188286A1 SG 2013013743 A SG2013013743 A SG 2013013743A SG 2013013743 A SG2013013743 A SG 2013013743A SG 188286 A1 SG188286 A1 SG 188286A1
Authority
SG
Singapore
Prior art keywords
cancer
dichloropyridin
compound
vinyl
pyrazol
Prior art date
Application number
SG2013013743A
Other languages
English (en)
Inventor
Benjamin Alan Diseroad
Original Assignee
Lilly Co Eli
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=44999860&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SG188286(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Lilly Co Eli filed Critical Lilly Co Eli
Publication of SG188286A1 publication Critical patent/SG188286A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
SG2013013743A 2010-10-05 2011-09-29 Crystalline (r) - (e) -2- (4- (2- (5- (1- (3, 5 -dichloropyridin-4 -yl) ethoxy) - 1h - indazol - 3 - yl) vinyl) -1 h- pyrazol- 1 -yl) ethanol and its use as fgfr inhibitor SG188286A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US38991110P 2010-10-05 2010-10-05
PCT/US2011/053798 WO2012047699A1 (en) 2010-10-05 2011-09-29 Crystalline (r) - (e) -2- (4- (2- (5- (1- (3, 5 -dichloropyridin-4 -yl) ethoxy) - 1h - indazol - 3 - yl) vinyl) -1 h- pyrazol- 1 -yl) ethanol and its use as fgfr inhibitor

Publications (1)

Publication Number Publication Date
SG188286A1 true SG188286A1 (en) 2013-04-30

Family

ID=44999860

Family Applications (1)

Application Number Title Priority Date Filing Date
SG2013013743A SG188286A1 (en) 2010-10-05 2011-09-29 Crystalline (r) - (e) -2- (4- (2- (5- (1- (3, 5 -dichloropyridin-4 -yl) ethoxy) - 1h - indazol - 3 - yl) vinyl) -1 h- pyrazol- 1 -yl) ethanol and its use as fgfr inhibitor

Country Status (35)

Country Link
US (1) US8530665B2 (ru)
EP (1) EP2625175B1 (ru)
JP (1) JP5940547B2 (ru)
KR (1) KR101527661B1 (ru)
CN (1) CN103153983B (ru)
AR (1) AR083091A1 (ru)
AU (1) AU2011312485B2 (ru)
BR (1) BR112013006336A2 (ru)
CA (1) CA2813329C (ru)
CL (1) CL2013000884A1 (ru)
CO (1) CO6710911A2 (ru)
DK (1) DK2625175T3 (ru)
DO (1) DOP2013000072A (ru)
EA (1) EA021817B1 (ru)
EC (1) ECSP13012539A (ru)
ES (1) ES2558777T3 (ru)
HK (1) HK1184147A1 (ru)
HR (1) HRP20151299T1 (ru)
HU (1) HUE026379T2 (ru)
IL (1) IL224850A (ru)
JO (1) JO3062B1 (ru)
MA (1) MA34552B1 (ru)
ME (1) ME02307B (ru)
MX (1) MX2013003907A (ru)
NZ (1) NZ608482A (ru)
PE (1) PE20140252A1 (ru)
PL (1) PL2625175T3 (ru)
PT (1) PT2625175E (ru)
RS (1) RS54457B1 (ru)
SG (1) SG188286A1 (ru)
SI (1) SI2625175T1 (ru)
TW (1) TWI418554B (ru)
UA (1) UA111725C2 (ru)
WO (1) WO2012047699A1 (ru)
ZA (1) ZA201301560B (ru)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19945982A1 (de) * 1999-09-24 2001-03-29 Knoll Ag Geschwindigkeitsbestimmte Partikel
WO2012088266A2 (en) 2010-12-22 2012-06-28 Incyte Corporation Substituted imidazopyridazines and benzimidazoles as inhibitors of fgfr3
PL3176170T3 (pl) 2012-06-13 2019-05-31 Incyte Holdings Corp Podstawione związki tricykliczne jako inhibitory fgfr
US9388185B2 (en) 2012-08-10 2016-07-12 Incyte Holdings Corporation Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors
US9266892B2 (en) 2012-12-19 2016-02-23 Incyte Holdings Corporation Fused pyrazoles as FGFR inhibitors
PT2986610T (pt) 2013-04-19 2018-03-09 Incyte Holdings Corp Heterociclos bicíclicos como inibidores de fgfr
CN103819396B (zh) * 2014-02-26 2016-06-15 四川大学 一种手性的1-(3,5-二氯吡啶-4-基)-乙醇的合成方法
US10851105B2 (en) 2014-10-22 2020-12-01 Incyte Corporation Bicyclic heterocycles as FGFR4 inhibitors
MA41551A (fr) 2015-02-20 2017-12-26 Incyte Corp Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4
WO2016134294A1 (en) 2015-02-20 2016-08-25 Incyte Corporation Bicyclic heterocycles as fgfr4 inhibitors
ES2751669T3 (es) 2015-02-20 2020-04-01 Incyte Corp Heterociclos bicíclicos como inhibidores FGFR
AR111960A1 (es) 2017-05-26 2019-09-04 Incyte Corp Formas cristalinas de un inhibidor de fgfr y procesos para su preparación
US11466004B2 (en) 2018-05-04 2022-10-11 Incyte Corporation Solid forms of an FGFR inhibitor and processes for preparing the same
KR20210018264A (ko) 2018-05-04 2021-02-17 인사이트 코포레이션 Fgfr 억제제의 염
WO2020185532A1 (en) 2019-03-08 2020-09-17 Incyte Corporation Methods of treating cancer with an fgfr inhibitor
KR20210142154A (ko) 2019-03-21 2021-11-24 옹쎄오 암 치료를 위한 키나제 억제제와 조합된 dbait 분자
US11591329B2 (en) 2019-07-09 2023-02-28 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
PE20221085A1 (es) 2019-10-14 2022-07-05 Incyte Corp Heterociclos biciclicos como inhibidores de fgfr
US11566028B2 (en) 2019-10-16 2023-01-31 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
US20220401436A1 (en) 2019-11-08 2022-12-22 INSERM (Institute National de la Santé et de la Recherche Médicale) Methods for the treatment of cancers that have acquired resistance to kinase inhibitors
CA3162010A1 (en) 2019-12-04 2021-06-10 Incyte Corporation Derivatives of an fgfr inhibitor
CA3163875A1 (en) 2019-12-04 2021-06-10 Incyte Corporation Tricyclic heterocycles as fgfr inhibitors
WO2021148581A1 (en) 2020-01-22 2021-07-29 Onxeo Novel dbait molecule and its use
CN111705099B (zh) * 2020-07-01 2022-03-08 天津药明康德新药开发有限公司 一种(s)-1-(3,5-二氯吡啶-4-取代)乙醇的制备方法
JP2023553835A (ja) * 2020-12-17 2023-12-26 ブロッサムヒル・セラピューティクス・インコーポレイテッド 大環状化合物およびそれらの使用
EP4352059A1 (en) 2021-06-09 2024-04-17 Incyte Corporation Tricyclic heterocycles as fgfr inhibitors

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6897231B2 (en) * 2000-07-31 2005-05-24 Signal Pharmaceuticals, Inc. Indazole derivatives as JNK inhibitors and compositions and methods related thereto
CA2421120C (en) 2000-09-11 2008-07-15 Chiron Corporation Quinolinone derivatives as tyrosine kinase inhibitors
KR20050004214A (ko) 2002-05-31 2005-01-12 에자이 가부시키가이샤 피라졸 화합물 및 이것을 포함하여 이루어지는 의약 조성물
BRPI0508895A (pt) * 2004-03-17 2007-09-11 Pfizer formas polimorficas e amorfa de {2-flúor-5-[3-((e)-2-piridn-2-il-vinil)-1h-indazol-6-ilamin]- fenil}-amida de ácido 2,5-dimetil-2h-pirazol-3-carboxìlico
JP4746299B2 (ja) * 2004-07-16 2011-08-10 ジュズ インターナショナル ピーティーイー エルティーディー 金属酸化物粉末の製造方法
JP2006163651A (ja) 2004-12-03 2006-06-22 Sony Computer Entertainment Inc 表示装置、表示装置の制御方法、プログラム及びフォントデータ
US20060160863A1 (en) * 2005-01-05 2006-07-20 Agouron Pharmaceuticals, Inc. Polymorphic and amorphous forms of 2-{3-[(E)-2-(4,6-dimethyl-pyridin-2-yl)-vinyl]-1H-indazol-6-ylamino}-N-(4-hydroxy-but-2-ynyl)benzamide
WO2007058626A1 (en) 2005-11-16 2007-05-24 S*Bio Pte Ltd Indazole compounds
NZ580126A (en) * 2007-04-05 2012-03-30 Pfizer Prod Inc Crystalline forms of 6- [2- (methylcarbamoyl) phenylsulfanyl] -3-e- [2- (pyridin-2-yl) ethenyl] indazole suitable for the treatment of abnormal cell growth in mammals
JO2860B1 (en) * 2009-05-07 2015-03-15 ايلي ليلي اند كومباني Phenylendazolyl compounds

Also Published As

Publication number Publication date
CL2013000884A1 (es) 2013-10-18
KR101527661B1 (ko) 2015-06-09
PT2625175E (pt) 2016-01-22
ME02307B (me) 2016-06-20
EP2625175B1 (en) 2015-11-18
HUE026379T2 (en) 2016-06-28
PE20140252A1 (es) 2014-03-12
CO6710911A2 (es) 2013-07-15
US20120083511A1 (en) 2012-04-05
CN103153983A (zh) 2013-06-12
IL224850A (en) 2016-09-29
JP5940547B2 (ja) 2016-06-29
NZ608482A (en) 2014-03-28
CA2813329C (en) 2015-05-26
EA201390275A1 (ru) 2013-07-30
JP2013538875A (ja) 2013-10-17
PL2625175T3 (pl) 2016-04-29
AU2011312485B2 (en) 2014-09-04
ZA201301560B (en) 2014-08-27
AR083091A1 (es) 2013-01-30
HRP20151299T1 (hr) 2016-01-01
WO2012047699A1 (en) 2012-04-12
DK2625175T3 (en) 2016-02-01
HK1184147A1 (en) 2014-01-17
AU2011312485A1 (en) 2013-03-07
CA2813329A1 (en) 2012-04-12
JO3062B1 (ar) 2017-03-15
RS54457B1 (en) 2016-06-30
BR112013006336A2 (pt) 2019-09-24
TW201249826A (en) 2012-12-16
EP2625175A1 (en) 2013-08-14
DOP2013000072A (es) 2013-08-15
TWI418554B (zh) 2013-12-11
ECSP13012539A (es) 2013-06-28
ES2558777T3 (es) 2016-02-08
KR20130052680A (ko) 2013-05-22
EA021817B1 (ru) 2015-09-30
SI2625175T1 (sl) 2016-01-29
UA111725C2 (uk) 2016-06-10
MX2013003907A (es) 2013-06-03
CN103153983B (zh) 2014-11-05
MA34552B1 (fr) 2013-09-02
US8530665B2 (en) 2013-09-10

Similar Documents

Publication Publication Date Title
EP2625175B1 (en) Crystalline (r)-(e)-2-(4-(2-(5-(1-(3,5-dichloropyridin-4-yl)ethoxy)-1h-indazol-3-yl)vinyl)-1h-pyrazol-1-yl)ethanol and its use as fgfr inhibitor
EP2427449B1 (en) Vinyl indazolyl compounds
EA018808B1 (ru) Ингибиторы протеинкиназы, фармацевтический состав на их основе и применение в терапии
TW202023559A (zh) 吡化合物及其用途
EP2531498B1 (en) Compounds and compositions as protein kinase inhibitors
EA038233B1 (ru) ДЕЙТЕРИРОВАННЫЕ СОЕДИНЕНИЯ ИМИДАЗО[4,5-c]ХИНОЛИН-2-ОНА И ИХ ПРИМЕНЕНИЕ В ЛЕЧЕНИИ РАКА
WO2020210381A1 (en) Heterocyclic compounds and uses thereof
WO2022213932A1 (zh) 吡咯并嘧啶酮类化合物及其应用
CN114761410B (zh) 吡咯并嘧啶酮类化合物及其应用
CN114539263B (zh) 一类含氮并杂环化合物及其药用组合物和应用
CN115315422B (zh) 酰胺类化合物及其用途
JP2022515622A (ja) チエノピリジノン化合物
CN116323582A (zh) 杂芳环类化合物及其用途